نتایج جستجو برای: viral gene delivery

تعداد نتایج: 1439069  

Journal: :Molecular therapy : the journal of the American Society of Gene Therapy 2018
Marta Holstein Cristina Mesa-Nuñez Csaba Miskey Elena Almarza Valentina Poletti Marco Schmeer Esther Grueso Juan Carlos Ordóñez Flores Dennis Kobelt Wolfgang Walther Manish K Aneja Johannes Geiger Halvard B Bonig Zsuzsanna Izsvák Martin Schleef Carsten Rudolph Fulvio Mavilio Juan A Bueren Guillermo Guenechea Zoltán Ivics

The Sleeping Beauty (SB) transposon system is a non-viral gene delivery platform that combines simplicity, inexpensive manufacture, and favorable safety features in the context of human applications. However, efficient correction of hematopoietic stem and progenitor cells (HSPCs) with non-viral vector systems, including SB, demands further refinement of gene delivery techniques. We set out to i...

2014
Yarong Liu Young Joo Kim Man Ji Jinxu Fang Natnaree Siriwon Li I Zhang Pin Wang

Adeno-associated virus type 2 (AAV2) is considered a promising gene delivery vector and has been extensively applied in several disease models; however, inefficient transduction in various cells and tissues has limited its widespread application in many areas of gene therapy. In this study, we have developed a general, but efficient, strategy to enhance viral transduction, both in vitro and in ...

2011
Chao Zhang Qing-Tao Wang He Liu Zhen-Zhu Zhang Wen-Lin Huang

Gene therapy is one of the most attractive fields in tumor therapy. In past decades, significant progress has been achieved. Various approaches, such as viral and non-viral vectors and physical methods, have been developed to make gene delivery safer and more efficient. Several therapeutic strategies have evolved, including gene-based (tumor suppressor genes, suicide genes, antiangiogenic genes...

Journal: :International journal of pharmaceutics 2012
Aliasger K Salem Siddhesh D Patil Diane J Burgess

A major goal of nucleic acid based therapies is to treat inherted and acquired disorders by adding, correcting, suppressing or eplacing genes (Abbas et al., 2008). Advantages of non-viral vectors or delivering nucleic acid based therapies include ease of scale-up, torage stability and improved quality control. The most promisng non-viral vectors have been liposomes and cationic polymers hich co...

Journal: :Circulation 2000
S A Nicklin S J White S J Watkins R E Hawkins A H Baker

BACKGROUND Gene transfer to vascular cells is a highly inefficient and nonselective process, defined by the lack of specific cell-surface receptors for both nonviral and viral gene delivery vectors. METHODS AND RESULTS We used filamentous phage display to isolate a panel of peptides that have the ability to bind selectively and efficiently to quiescent human umbilical vein endothelial cells (...

Fariba Sadeghi Mina Eghbali Reza Golijani Moghadam

Today, it has been confirmed that the viral infections play an important role in premature delivery and abortion. This study was carried out to determine the frequency rate of papilloma virus types 16 and 18 in pregnant women and their relationship with premature delivery and abortion. In this study, vaginal secretions were collected from pregnant women who had been referred to the women clinic...

Journal: :the iranian journal of pharmaceutical research 0
bahram kazemi shahid beheshti university of medical sciences amir zarebkohan biomedical engineering and medical physics department, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran farhood najafi department of resin and additives, institute for color science and technology, tehran, iran hamid reza moghimi school of pharmacy, shahid beheshti university of medical sciences, tehran, iran mohammad hemmati biomedical engineering and medical physics department, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran mohammad reza deevband biomedical engineering and medical physics department, faculty of medicine, shahid beheshti university of medical sciences, tehran, iran

glioma, as a primary tumor of central nervous system, is the main cause of death in patients with brain cancer. therefore, development of an efficient strategy for treatment of glioma is worthy. the aim of the current study was to develop a srl peptide-coated dendrimer as a novel dual gene delivery system for targeting the lrp receptor, an up-regulated gene in both bbb and glioma cells. to perf...

Journal: :Proceedings of the National Academy of Sciences of the United States of America 1998
M A Morsy M Gu S Motzel J Zhao J Lin Q Su H Allen L Franlin R J Parks F L Graham S Kochanek A J Bett C T Caskey

Adenoviral (Ad)-mediated in vivo gene transfer and expression are limited in part by cellular immune responses to viral-encoded proteins and/or transgene immunogenicity. In an attempt to diminish the former responses, we have previously developed and described helper-dependent (HD) Ad vectors in which the viral protein coding sequences are completely eliminated. These HD vectors have up to 37 k...

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